Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 18
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17